Add curved arrow(s) to draw step 1 of the mechanism. H₂C CH₂ the CH₂ H₂C ÕH Save for Later Q-CH, CH₂ CH, CH₁ CH₂ + H₂C H,C a Edit Drawing CH, Ind A
Reactive Intermediates
In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.
Hydride Shift
A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.
Vinylic Carbocation
A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.
Cycloheptatrienyl Cation
It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.
Stability of Vinyl Carbocation
Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.
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![Add curved arrow(s) to draw step 1 of the mechanism.
H₂C
H₂C
CH₂
CH
Save for Later
CH₂
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ÖH
H.C.
OCH,
CH₂
CH₂
CH,
CH₁
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CH₂
H₂C
XX
H₂C
H₂C
CH,
O–CH,
CH
CH₂](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F84a1b519-852c-4c6f-9ec3-1652ee1dd237%2F5068aca9-8b4d-4871-807d-b1bb728a5bb6%2Fnguo05q_processed.jpeg&w=3840&q=75)
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